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Mirror Medacta Shoulder System Pivotal Trial

NCT05062252 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2025-05-08

No results posted yet for this study

Summary

The purpose of this study is to demonstrate safety and efficacy of the Mirror Medacta Shoulder System in total shoulder arthroplasty.

Conditions

  • Arthritis Shoulder
  • Post-traumatic Arthrosis of Other Joints, Upper Arm

Interventions

DEVICE

Mirror Medacta Shoulder System

Anatomic total shoulder arthroplasty system

DEVICE

Medacta Shoulder System

Anatomic total shoulder arthroplasty system - standard configuration

Sponsors & Collaborators

  • Medacta International SA

    lead INDUSTRY

Principal Investigators

  • Matthias A Zumstein, Prof Dr. med · Lindenhofgruppe AG (Bern)

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-01-05
Primary Completion
2026-12-30
Completion
2027-12-30

Countries

  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05062252 on ClinicalTrials.gov